IMMY, Inc.
United States Last updated 25 Oct 2026
- Devices
- 6
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Mycobacterium Digestion and Decontamination Reagent Sets Ref TBRP30-60
Mycobacterium Digestion and Decontamination Reagent Sets Ref TBPN67-60
About
Fungal Diagnostics for a Healthier Tomorrow. IMMY raises global healthcare standards through rapid, reliable, and accessible solutions.
What IMMY, Inc. makes
IMMY, Inc. manufactures Mycobacterium Digestion and Decontamination Reagent Sets, including the MycoDDR Trident variant, designed for processing and decontaminating mycobacterial samples in laboratory settings.
These reagent sets are classified as Class A medical devices and are registered in the EU’s eudamed database. The company is based in the United States.
Frequently asked questions
How many devices does IMMY, Inc. have in the registry?
The registry currently lists 6 devices for IMMY, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list IMMY, Inc.'s devices?
Among its 6 most recently registered devices, IMMY, Inc. has devices listed in EUDAMED (6 devices).
What risk classes do IMMY, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for IMMY, Inc.'s devices are IVDR Class A. Each device page shows its own class and authorisation.
What are the newest devices from IMMY, Inc. in the registry?
The most recently registered devices listed for IMMY, Inc. include Mycobacterium Digestion and Decontamination Reagent Sets, MycoDDR Trident Mycobacterium Digestion and Decontamination Reagent Sets and MycoDDR™ Trident™ Mycobacterium Digestion and Decontamination Reagent Sets.
Information
- Address
- 2701, Corporate Centre Dr, Norman, United States
- Website
- www.immy.com
- [email protected]
- PRRC contact
- Hunter Conover
- EUDAMED SRN
- US-MF-000025165
- FDA FEI number
- 1627497